化学学报 ›› 1987, Vol. 45 ›› Issue (6): 613-615. 上一篇    下一篇

研究论文

4-取代-2,6-二(羟甲基)苯酚的选择氧化

胡跃飞;胡宏纹   

  1. 南京大学化学系
  • 发布日期:1987-06-15

Selective oxidation of 4-substituted-2,6-di(hydroxymethylphenols

HU YUEFEI;HU HONGWEN   

  • Published:1987-06-15

关键词: 苯酚 P, 苯酚 P, 苯甲醛 P, 氧化, 三乙胺 P, 选择性, 溴化物, 镁化合物, 羟甲基, 羟甲基

4-Substituted-2,6-bis(hydroxymethyl)phenols were converted to their magnesium salts with ethylmagnesium bromide and then treated with paraformaldehyde to give the corresponding 5-substituted-2-hydroxy-3-hydroxymethyl benzaldehydes. Further oxidation of the second hydroxymethyl group in these products was prevented by the prior formation of an electron-withdrawing formyl group. Thus, benzyl alcs. I (R = Br, Cl, Me, MeO, Ph, R1 = R2 = H; R = Cl, R1 = R2 = Me) gave 75-88% benzaldehydes II.

Key words: PHENOL P, PHENOL P, BENZALDEHYDE P, OXIDATION, TRIETHYL AMINE P, SELECTIVITY, BROMIDE, MAGNESIUM COMPOUNDS, CARBINOL GROUP, CARBINOL GROUP

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